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Benzoic acid, 4-(1H-tetrazol-5-yl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88010-91-7

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88010-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88010-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,1 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88010-91:
(7*8)+(6*8)+(5*0)+(4*1)+(3*0)+(2*9)+(1*1)=127
127 % 10 = 7
So 88010-91-7 is a valid CAS Registry Number.

88010-91-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-(2H-tetrazol-5-yl)benzoate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88010-91-7 SDS

88010-91-7Relevant academic research and scientific papers

Preparation and reactions of (1 H-tetrazol-5-yl)zinc pivalates

Tüllmann, Carl Phillip,Steiner, Sebastian,Knochel, Paul

, p. 2357 - 2363 (2020/08/19)

The preparation and reactivity of new solid heterocyclic organozinc reagents, namely N -protected (1 H -tetrazol-5-yl)zinc pivalates, as storable solids with appreciably air and moisture stability are reported. They are obtained in high yields from protected 1 H -tetrazoles by de-protonation using the mixed zinc-magnesium base TMPZnCl·Mg(OPiv) 2(abbreviated as TMPZnOPiv; TMP = 2,2,6,6-tetramethylpiperidyl). Subsequent cross-couplings and copper-catalyzed electrophilic aminations using hydroxylamine benzoates give access to functionalized 1 H -tetrazoles while tolerating many functional groups.

HETEROCYCLIC COMPOUNDS AS INHIBITORS OF MONOACYLGLYCEROL LIPASE (MAGL)

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Page/Page column 219, (2020/10/21)

The application relates to heterocyclic compounds of the general formula (I), compositions comprising such compounds, a process for preparing these compounds and their medical use. The compounds act as monoacylglycerol lipase (MAGL) inhibitors and are useful in the treatment of neuroinflammation, neurodegenerative diseases, pain, cancer or mental disorders.

Facile one-pot preparation of 5-aryltetrazoles and 3-arylisoxazoles from aryl bromides

Kobayashi, Eiji,Togo, Hideo

, p. 4226 - 4235 (2018/07/06)

The successive treatment of aryl bromides with n-BuLi, DMF, hydroxylamine hydrochloride, and finally diphenylphosphoryl azide provided efficiently the corresponding 5-aryltetrazoles in good to moderate yields. Similarly, the successive treatment of aryl bromides with n-BuLi, DMF, hydroxylamine hydrochloride, and finally diethyl acetylenedicarboxylate and Oxone provided efficiently the corresponding diethyl 3-arylisoxazole-4,5-dicarboxylates in good to moderate yields. Aromatic aldoximes are the key intermediates in both reactions, and 5-aryltetrazoles and 3-arylisoxazoles could be obtained from aryl bromides in one pot under transition-metal-free conditions.

Promoting near-infrared emission of neodymium complexes by tuning the singlet and triplet energy levels of β-diketonates

Yang, Lifen,Gong, Zeliang,Nie, Daobo,Lou, Bin,Bian, Zuqiang,Guan, Min,Huang, Chunhui,Lee, Hyun Joo,Baik, Woo Phil

, p. 791 - 796 (2007/10/03)

A series of neodymium complexes with various modified β-diketonates and their corresponding gadolinium complexes have been synthesized and characterized. The singlet and triplet energy levels of the coordinated ligands were measured and compared. These co

5-Aryltetrazole Compounds, compositions thereof, and uses therefor

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Page 30, (2008/06/13)

The present invention relates to 5-Aryltetrazole compounds, compositions comprising a 5-Aryltetrazole compound, and methods for treating an inflammation disease, a reperfusion disease, hyperuricemia, gout, or tumor-lysis syndrome in an animal in need ther

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